Follicular helper-like γδ T cells promote plasma cell differentiation in Behçet’s disease

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Authors: Sahar Shaaban Mohammed, Abdullah Khalifah S. Alkhalifah, Rahilah Mirza, Sarah-Pristine Omoefe Okinedo, Rani Aishwarya Inampudi, Azimoon Bibi, Amal Senusi, Claire Pardieu, Neil E. McCarthy, F. Fortune, Fabian Flores‐Borja
Cited by: 2
References: 51

Abstract

Objectives Behçet’s disease (BD) is a systemic vasculitis characterized by recurrent oral and genital ulcers. The disease can manifest diverse phenotypes -such as mucocutaneous, ocular BD- with an uncertain role for autoantibodies in disease pathogenesis. Altered γδT-cell and B-cell phenotypes have been widely reported in BD, but it remains unknown whether these lineages can interact to promote autoantibody production. Methods This study included 75 patients with a BD diagnosis, alongside 41 healthy control (HC) volunteers. We performed ex vivo flow-cytometric profiling of blood γδT and B cells, established a cell culture system to investigate plasma cell generation in vitro , and quantified anti-HSP60 autoantibody levels in BD and HC participants’ serum and cell culture supernatants. Results BD patients with active disease displayed a significant increase in the frequency of cells CXCR5 + PD-1 + Vδ2 T cells resembling a follicular helper-like functional state. Upon stimulation, Vδ2 T cells from BD patients showed increased expression of ICOS and CXCR5, induced significant B cell proliferation, and promoted differentiation of plasma cells in vitro . Cultures of cells from BD patients contained increased levels of multiple cytokines that can support plasma cell differentiation (IL-4, IL-10, IL-17, CXCL13, TNF-α, IFN-γ). Anti-HSP60 autoantibodies were significantly enriched in blood serum from BD patients with active disease as well as the supernatants of patient-derived cell cultures compared to the healthy volunteer cell cultures. Conclusion Our findings suggest that γδT cells may enhance B-cell differentiation into antibody-producing plasma cells in BD patients with mucocutaneous and ocular clinical phenotypes.

Fields of Study & Subjects

Ocular Diseases and Behçet’s Syndrome Vasculitis and related conditions Otitis Media and Relapsing Polychondritis

Publication details

Journal / source
Frontiers in Immunology
Publisher
Frontiers Media SA
Volume
17
Pages
1763174–1763174
Publication date
9 February 2026
Language
EN